Canonical Allele Identifier: CA396938626
Gene: SLC38A8 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.84065519G>T (hg19) chr16:g.84031914G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031914G>T , CM000678.2:g.84031914G>T GRCh38
NC_000016.9:g.84065519G>T , CM000678.1:g.84065519G>T GRCh37
NC_000016.8:g.82623020G>T NCBI36
NG_034136.1:g.15244C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.585C>A MANE Select ENSP00000299709.3:p.Tyr195Ter
ENST00000299709.7:c.585C>A ENSP00000299709.3:p.Tyr195Ter
ENST00000568178.1:c.585C>A ENSP00000457737.1:p.Tyr195Ter
NM_001080442.2:c.585C>A NP_001073911.1:p.Tyr195Ter
XM_011522872.1:c.585C>A XP_011521174.1:p.Tyr195Ter
XM_017022946.1:c.585C>A XP_016878435.1:p.Tyr195Ter
NM_001080442.3:c.585C>A MANE Select NP_001073911.1:p.Tyr195Ter
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